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An experimental treatment for ALS caused by mutations in a specific gene called CHCHD10 showed promise in one person, a study reports.

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An experimental treatment for ALS caused by mutations in a specific gene called CHCHD10 showed promise in one person, a study reports.
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A team of U.S. scientists says measuring blood levels of toxic TDP-43 protein may help diagnose ALS, speeding what's now a lengthy process.
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Columnist Kristin Neva shares how her husband, Todd, seems to emotionally focus less on ALS and being paralyzed than he previously did.
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Disease history was linked to higher ALS risk, while better cardiovascular health was associated with lower risk in a large UK study.
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We are all adapting to modern life, writes columnist Dagmar Munn, who says changes made to navigate ALS sometimes mirror cultural shifts.
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Common viral infections such as influenza and COVID-19 may accelerate the onset and progression of ALS, a new mouse study suggests.
The ALS community is mourning the loss of advocate Brooke Eby, who passed away Oct. 1 at age 37.
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Strength can exist without movement, effort, or action.
#ALScommunity
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For people with neuromuscular diseases at MDA Engage: Chicago, the biggest takeaway was realizing they are not alone.
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Guest writer Cristy Hardin shares how defining friendship took on new meaning when she became a caregiver for a close friend.
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Medicinova completed the last patient visit in the placebo-controlled portion of a trial testing MN-166, its experimental treatment for ALS.
Today holds space for you exactly as you are.
#ALSCommunity
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Advocates are cheering as legislation to renew the ACT for ALS headed to President Trump's desk days before the program is set to expire.
Kiersten, who lives with Friedreich’s ataxia (FA), speaks to that unseen exhaustion and why understanding from others can matter.
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A walk past fruit trees reminds columnist Kristin Neva of her father, and she thinks about what will remind her children of their dad.
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Early rehabilitation and a care team that works together are crucial for helping people with neuromuscular disease stay active and safe.
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Voice Back, an AI app, helps people with ALS and other causes of speech loss communicate using a voice that sounds like their own.
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A progressive decline in lung function is unavoidable in ALS, but there are steps that patients can take to improve breathing issues.
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Low muscle mass in the arms and legs and sarcopenia were linked to poorer survival in people with ALS in a small prospective study.
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Columnist Kristin Neva takes note of the changing seasons with an initial sense of dread, then refocuses on the good things that also come.